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Präparative Enantiomerentrennung einer Chroman-2-carbonsäure durch Chromatographie von Glucose-Derivaten

✍ Scribed by Netscher, Thomas ;Gautschi, Iwan


Publisher
John Wiley and Sons
Year
1992
Tongue
English
Weight
470 KB
Volume
1992
Category
Article
ISSN
0947-3440

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✦ Synopsis


Preparative Separation of the Enantiomers of a Chroman‐2‐carboxylic Acid via Chromatography of Glucose Derivatives

Starting from the commercially available racemic carboxylic acid 2a, b (S)‐Trolox methyl ether (1a), useful as a chiral reagent for capillary gas chromatography and supercritical fluid chromatography, was obtained in enantiomerically pure form (e.e. >99.9%) by the separation of esters derived from diacetone D‐glucose and subsequent saponification.